Impact of L-carnitine on plasma lipoprotein(a) concentrations: A systematic review and meta-analysis of randomized controlled trials

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作者
Maria-Corina Serban
Amirhossein Sahebkar
Dimitri P. Mikhailidis
Peter P. Toth
Steven R. Jones
Paul Muntner
Michael J. Blaha
Florina Andrica
Seth S. Martin
Claudia Borza
Gregory Y. H. Lip
Kausik K. Ray
Jacek Rysz
Stanley L. Hazen
Maciej Banach
机构
[1] University of Alabama at Birmingham,Department of Epidemiology
[2] Discipline of Pathophysiology,Department of Functional Sciences
[3] “Victor Babes” University of Medicine and Pharmacy,Department of Clinical Biochemistry
[4] Biotechnology Research Center,Department of Primary Care and Public Health
[5] Mashhad University of Medical Sciences,Department of Hypertension
[6] Metabolic Research Centre,Department for Cellular and Molecular Medicine
[7] Royal Perth Hospital,undefined
[8] School of Medicine and Pharmacology,undefined
[9] University of Western Australia,undefined
[10] Royal Free Campus,undefined
[11] University College London Medical School,undefined
[12] University College London (UCL),undefined
[13] Preventive Cardiology,undefined
[14] CGH Medical Center,undefined
[15] The Johns Hopkins Ciccarone Center for the Prevention of Heart Disease,undefined
[16] Faculty of Pharmacy,undefined
[17] Discipline of Pharmaceutical Chemistry “Victor Babes” University of Medicine and Pharmacy,undefined
[18] University of Birmingham Centre for Cardiovascular Sciences,undefined
[19] City Hospital,undefined
[20] School of Public Health,undefined
[21] Imperial College London,undefined
[22] Chair of Nephrology and Hypertension,undefined
[23] Medical University of Lodz,undefined
[24] Lerner Research Institute,undefined
[25] Cleveland Clinic,undefined
来源
Scientific Reports | / 6卷
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摘要
We aimed to assess the impact of L-carnitine on plasma Lp(a) concentrations through systematic review and meta-analysis of available RCTs. The literature search included selected databases up to 31st January 2015. Meta-analysis was performed using fixed-effects or random-effect model according to I2 statistic. Effect sizes were expressed as weighted mean difference (WMD) and 95% confidence interval (CI). The meta-analysis showed a significant reduction of Lp(a) levels following L-carnitine supplementation (WMD: −8.82 mg/dL, 95% CI: −10.09, −7.55, p < 0.001). When the studies were categorized according to the route of administration, a significant reduction in plasma Lp(a) concentration was observed with oral (WMD: −9.00 mg/dL, 95% CI: −10.29, −7.72, p < 0.001) but not intravenous L-carnitine (WMD: −2.91 mg/dL, 95% CI: −10.22, 4.41, p = 0.436). The results of the meta-regression analysis showed that the pooled estimate is independent of L-carnitine dose (slope: −0.30; 95% CI: −4.19, 3.59; p = 0.878) and duration of therapy (slope: 0.18; 95% CI: −0.22, 0.59; p = 0.374). In conclusion, the meta-analysis suggests a significant Lp(a) lowering by oral L-carnitine supplementation. Taking into account the limited number of available Lp(a)-targeted drugs, L-carnitine might be an effective alternative to effectively reduce Lp(a). Prospective outcome trials will be required to fully elucidate the clinical value and safety of oral L-carnitine supplementation.
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